Skip to content

Low-Dose Ketamine in Children With ADNP Syndrome

A Phase 2A Open-Label Study Evaluating the Safety and Efficacy of Low-Dose Ketamine in Children With ADNP Syndrome

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04388774
Enrollment
10
Registered
2020-05-14
Start date
2020-08-19
Completion date
2021-06-08
Last updated
2023-07-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ADNP Syndrome

Keywords

Ketamine, ADNP, Activity-Dependent Neuroprotector Protein, Chromosome Disorders, Chromosome Aberrations

Brief summary

This is a Phase 2A, single dose, open-label study to evaluate the safety, tolerability, and efficacy of a low-dose, 40-minute infusion into the veins (intravenous infusion or IV) of ketamine in children with ADNP syndrome (Activity-Dependent Neuroprotective Protein). The study team will enroll 10 participants, ages 5 to 12, at Mount Sinai. The study participation is expected to last 4 weeks and will include 5 scheduled clinic visits in order to complete safety monitoring, clinical assessments, and biomarker collection. At the conclusion of this study, the study team expects to demonstrate the safety and tolerability of low-dose ketamine in children with ADNP syndrome. Additionally, the study team anticipates identifying meaningful signals of efficacy in clinical outcome measures using RNA and DNA sequencing to analyze ADNP protein expression and DNA methylation profiles, a natural process by which methyl groups are added to the DNA to change its activity, in order to assess sensitivity to change with low-dose ketamine treatment and inform future phase 3 studies. Ketamine is not currently approved by the Food and Drug Administration to treat this syndrome, but it is approved for use in children in other situations, for example in anesthesia.

Interventions

DRUGKetamine

A single 40-minute intravenous infusion

Sponsors

Alexander Kolevzon
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
5 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* 5 to 12 years old (inclusive) at the time of informed consent; * Has a diagnosis of ADNP syndrome, confirmed by genetic testing prior to subject randomization; * Has a Clinical Global Impression-Severity score of 4 (moderately ill) or greater at screening; * Any concomitant medication, including anti-epileptic and/or behavioral medications, supplements, and special diets, must be at a stable dose for at least 4 weeks before; * Has an English-speaking caregiver capable of providing informed consent and able to attend all scheduled study visits, oversee the administration of study drug, and provide feedback regarding the subject's behavior and other symptoms as described in the protocol; * Provide assent to the protocol (when applicable); * Has a caregiver who will agree not to post any of the subject's personal medical data related to the study or information related to the study on any website or social media site (e.g., Facebook and Twitter) until they have been notified that the study is completed. * Age-specific blood pressure parameters for inclusion in the study will be based on established guidelines.

Exclusion criteria

* Has a concomitant disease (e.g., gastrointestinal, renal, hepatic, endocrine, respiratory, or cardiovascular system disease) or condition or any clinically significant finding at screening that could interfere with the conduct of the study or that would pose an unacceptable risk to the subject in this study; * Has clinically significant lab abnormalities or vital signs at the time of screening (e.g., alanine aminotransferase or aspartate aminotransferase \>2.5 × upper limit of normal; total bilirubin or creatinine \>1.5 × upper limit of normal). Re-testing of safety labs is allowed; * Hypertension that is not well controlled (systolic BP \>130-140 mm Hg or diastolic BP \>85-95 mm Hg depending on age); * A blood pressure reading over 160/90 or two separate readings over 140/90 at screening or baseline visits; * Thyroid impairment, as reflected by a TSH \> 4.2 mU/L; * Cardiac disease, as reflected by an EKG that is abnormal and of concern for cardiac disease; * Has had changes in his/her medication regimen within the previous month; * Has a history of uncontrollable seizure disorder or seizure episodes within 1 month of screening; * Has a history of suicidal behavior or considered by the investigator to be at high risk of suicide; * Has a current or past history of psychotic symptoms; * Has enrolled in any clinical trial or used of any investigational agent, device, and/or investigational procedure within the 30 days before screening or does so concurrently with this study.

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants With an Adverse EventWeek 4Number of Participants with an adverse event as defined by the Systematic Longitudinal Assessment of Adverse Events (SLAES) which is a comprehensive form that assesses medical and behavioral conditions that were present at screening and/or baseline. Conditions are considered treatment emergent if their severity increased significantly after the participant had taken at least one dose of the study treatment. Treatment emergent adverse events will be tracked considered in the adverse event safety analysis. Severity of adverse events are categorized as mild, moderate, severe, life-threatening, or resulting in death and the treating physician indicates if the adverse event was related or unrelated to study drug.

Secondary

MeasureTime frameDescription
Anxiety, Depression and Mood Scales (ADAMS)Baseline and Week 1The ADAMS is a parent/caregiver-completed measure and consists of 28 items, grouped into five subscales (Manic/Hyperactive Behavior, Depressed Mood, Social Avoidance, General Anxiety, Obsessive Behavior), and scored on a four-point Likert scale that combines frequency and severity ratings from 0-3. Subscales range - Hyperactivity 0-15; Depressed 0-21; Social Avoidance 0-21; General anxiety 0-21; OCD 0-9. Scores are not summed. Higher score indicates poorer health outcomes.
Repetitive Behavior Scale-Revised (RBS-R)Baseline, Week 1Change in repetitive behaviors at weeks 1 compared to baseline. RBS-R subscales - Stereo 0-18; Self injury 0-24; Compulsive 0-24; Ritualistic 0-18; Sameness 0-33; Restricted 0-12. Total scale range from 0 to 126 with higher score indicating worse health outcomes.
Clinical Global Impressions - Improvement Scale (CGI-I)Baseline, Week 2, and Week 4Changes in scale at weeks 2, and 4 compared to baseline. Clinical Global impressions - Improvement Scale is anchored to symptoms of ADNP syndrome for the assessment of treatment effects. CGI-I total score from 1 to 7 point scale, with higher score indicating worse health outcomes.
Childrens Sleep Habits QuestionnaireBaseline, Week 1Change in sleep habits at week 1 compared to baseline. Full scale from 0 to 110, with higher score indicating worse health outcomes.
Peabody Picture Vocabulary Test and Expressive Vocabulary TestBaseline, Week 1, Week 2, and Week 4Expressive and receptive language assessed by Peabody Picture Vocabulary Test and Expressive Vocabulary Test at Day 1, Weeks 1, 2, and 4. Full scale from 40 to 160, with higher score indicating better health outcomes.
Aberrant Behavior ChecklistBaseline, Week 1Changes in scale at week 1 compared to baseline. Aberrant Behavior Checklist is a behavior rating scale for the assessment of treatment effects. Each item is scored as 0 (never a problem), 1 (slight problem), 2 (moderately serious problem), or 3 (severe problem). Subscales from 0-45 for Irritability; 0-48 for Social Withdrawal and Hyperactivity; from 0-21 for Stereotypy; and 0-12 for In Speech , with total scale from 0 to 48, with higher score indicating worse health outcomes.
Latency to First SaccadeBaseline, Day 1, Week 1Change at week 1, week 2, and week 4 as compared to baseline using computerized eye tracking to record where the subject is looking during an activity in which the subject will see different social and non-social stimuli. Latency to first saccade to the target
Proportion of Target-DwellingBaseline, Day 1, Week 1Change at Day 1 and Week 1 as compared to baseline using computerized eye tracking to record where the subject is looking during an activity in which the subject will see different social and non-social stimuli. Proportion of time participants spent dwelling on the target versus distractor.
Electrophysiology RecordingBaseline, Week 1, Week 2, and Week 4Electroencephalographic recordings to measure Auditory Event Related Potentials at baseline, week 1, week 2, and week 4. In separate blocks, participants heard a 500-ms click at either a stimulation rate of 40 or 20 Hz. Click trains were presented 150 times each, with an intertrial interval of 50 ms, at approximately 60 db. Higher number indicates higher amplitude neural response to auditory stimuli.
Vineland Adaptive Behavior ScalesBaseline and Week 4Changes in scale at week 4 compared to baseline. Vineland Adaptive Behavior Scales measures adaptive functioning. Higher score indicating better health outcomes. Domain scores are standard scores - population mean 100 standard deviation 15. an overall composite score, it consists of three subscales: (a) communication (receptive, expressive, written), (b) socialization (interpersonal relationships, play and leisure, coping skills), and (c) daily living (person, domestic, community).
Caregiver Strain Questionnaire (CGSQ)Baseline and Week 1Caregiver Strain Questionnaire (CGSQ) is a 13 question tool, with a 5-point Likert scale ranging from Not at all (0) to Very much (4). Domains (Objective strain, Subjective externalized strain, Subjective internalized strain) are averaged scores, range from 0-4. Total score (Global score) is a sum of the three subdomains. Full scale range 0-12, higher score indicates more severe strain.
Proportion of Target-First Trials SaccadesBaseline, Day 1, Week 1Change at Day 1 and Week 1 as compared to baseline using computerized eye tracking to record where the subject is looking during an activity in which the subject will see a video of a person with two objects, turning her head towards one of the objects, the target. Mean proportion of trials in which participants made saccades to the target before the distractor.

Countries

United States

Participant flow

Recruitment details

Ten participants were screened, and all met criteria for inclusion and were enrolled between August 2020 and May 2021.

Participants by arm

ArmCount
Ketamine
Single-dose (0.5 mg/kg) infused intravenously over 40 minutes
10
Total10

Baseline characteristics

CharacteristicKetamine
Age, Continuous9.50 years
STANDARD_DEVIATION 2.3
Developmental quotient
FSDQ - full scale developmental quotient
28.81 quotient
STANDARD_DEVIATION 15.42
Developmental quotient
NVDQ - nonverbal developmental quotient
31.28 quotient
STANDARD_DEVIATION 16.13
Developmental quotient
VDQ - verbal developmental quotient
26.71 quotient
STANDARD_DEVIATION 15.33
Genetic mutation
Frameshift
6 Participants
Genetic mutation
Nonsense
4 Participants
Number of Participants with ADHD7 Participants
Number of Participants with ASD4 Participants
Race/Ethnicity, Customized
Hispanic/Latino
2 Participants
Race/Ethnicity, Customized
White
8 Participants
Sex: Female, Male
Female
3 Participants
Sex: Female, Male
Male
7 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 10
other
Total, other adverse events
9 / 10
serious
Total, serious adverse events
0 / 10

Outcome results

Primary

Number of Participants With an Adverse Event

Number of Participants with an adverse event as defined by the Systematic Longitudinal Assessment of Adverse Events (SLAES) which is a comprehensive form that assesses medical and behavioral conditions that were present at screening and/or baseline. Conditions are considered treatment emergent if their severity increased significantly after the participant had taken at least one dose of the study treatment. Treatment emergent adverse events will be tracked considered in the adverse event safety analysis. Severity of adverse events are categorized as mild, moderate, severe, life-threatening, or resulting in death and the treating physician indicates if the adverse event was related or unrelated to study drug.

Time frame: Week 4

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
KetamineNumber of Participants With an Adverse Event9 Participants
Secondary

Aberrant Behavior Checklist

Changes in scale at week 1 compared to baseline. Aberrant Behavior Checklist is a behavior rating scale for the assessment of treatment effects. Each item is scored as 0 (never a problem), 1 (slight problem), 2 (moderately serious problem), or 3 (severe problem). Subscales from 0-45 for Irritability; 0-48 for Social Withdrawal and Hyperactivity; from 0-21 for Stereotypy; and 0-12 for In Speech , with total scale from 0 to 48, with higher score indicating worse health outcomes.

Time frame: Baseline, Week 1

Population: Each participant had one caregiver provide rated assessments.

ArmMeasureGroupValue (MEAN)Dispersion
KetamineAberrant Behavior ChecklistSocial withdrawal9.9 score on a scaleStandard Deviation 8.96
KetamineAberrant Behavior ChecklistHyperactivity24.5 score on a scaleStandard Deviation 14.66
KetamineAberrant Behavior ChecklistMotor stereotypies7.8 score on a scaleStandard Deviation 5.31
KetamineAberrant Behavior ChecklistInappropriate speech3.6 score on a scaleStandard Deviation 2.88
KetamineAberrant Behavior ChecklistIrritability20.5 score on a scaleStandard Deviation 13.33
Caregiver Rated Assessment at 1 WeekAberrant Behavior ChecklistInappropriate speech3.3 score on a scaleStandard Deviation 2.21
Caregiver Rated Assessment at 1 WeekAberrant Behavior ChecklistIrritability10.9 score on a scaleStandard Deviation 10.6
Caregiver Rated Assessment at 1 WeekAberrant Behavior ChecklistSocial withdrawal4.2 score on a scaleStandard Deviation 4.96
Caregiver Rated Assessment at 1 WeekAberrant Behavior ChecklistMotor stereotypies4.5 score on a scaleStandard Deviation 3.66
Caregiver Rated Assessment at 1 WeekAberrant Behavior ChecklistHyperactivity16.2 score on a scaleStandard Deviation 13.35
Secondary

Anxiety, Depression and Mood Scales (ADAMS)

The ADAMS is a parent/caregiver-completed measure and consists of 28 items, grouped into five subscales (Manic/Hyperactive Behavior, Depressed Mood, Social Avoidance, General Anxiety, Obsessive Behavior), and scored on a four-point Likert scale that combines frequency and severity ratings from 0-3. Subscales range - Hyperactivity 0-15; Depressed 0-21; Social Avoidance 0-21; General anxiety 0-21; OCD 0-9. Scores are not summed. Higher score indicates poorer health outcomes.

Time frame: Baseline and Week 1

ArmMeasureGroupValue (MEAN)Dispersion
KetamineAnxiety, Depression and Mood Scales (ADAMS)Hyperactivity10.1 score on a scaleStandard Deviation 4.23
KetamineAnxiety, Depression and Mood Scales (ADAMS)General anxiety6.3 score on a scaleStandard Deviation 5.96
KetamineAnxiety, Depression and Mood Scales (ADAMS)Social avoidance6.1 score on a scaleStandard Deviation 4.23
KetamineAnxiety, Depression and Mood Scales (ADAMS)Obsessive/compulsive2.5 score on a scaleStandard Deviation 2.01
KetamineAnxiety, Depression and Mood Scales (ADAMS)Depressed2.6 score on a scaleStandard Deviation 3.31
Caregiver Rated Assessment at 1 WeekAnxiety, Depression and Mood Scales (ADAMS)Obsessive/compulsive1.6 score on a scaleStandard Deviation 1.51
Caregiver Rated Assessment at 1 WeekAnxiety, Depression and Mood Scales (ADAMS)Depressed2.1 score on a scaleStandard Deviation 2.69
Caregiver Rated Assessment at 1 WeekAnxiety, Depression and Mood Scales (ADAMS)Hyperactivity6.7 score on a scaleStandard Deviation 3.5
Caregiver Rated Assessment at 1 WeekAnxiety, Depression and Mood Scales (ADAMS)Social avoidance3.5 score on a scaleStandard Deviation 3.47
Caregiver Rated Assessment at 1 WeekAnxiety, Depression and Mood Scales (ADAMS)General anxiety4.3 score on a scaleStandard Deviation 4.74
Secondary

Caregiver Strain Questionnaire (CGSQ)

Caregiver Strain Questionnaire (CGSQ) is a 13 question tool, with a 5-point Likert scale ranging from Not at all (0) to Very much (4). Domains (Objective strain, Subjective externalized strain, Subjective internalized strain) are averaged scores, range from 0-4. Total score (Global score) is a sum of the three subdomains. Full scale range 0-12, higher score indicates more severe strain.

Time frame: Baseline and Week 1

ArmMeasureGroupValue (MEAN)Dispersion
KetamineCaregiver Strain Questionnaire (CGSQ)Objective strain2.79 score on a scaleStandard Deviation 1.11
KetamineCaregiver Strain Questionnaire (CGSQ)Subjective externalized strain2.18 score on a scaleStandard Deviation 1.11
KetamineCaregiver Strain Questionnaire (CGSQ)Subjective internalized strain3.3 score on a scaleStandard Deviation 1.15
KetamineCaregiver Strain Questionnaire (CGSQ)Global score8.27 score on a scaleStandard Deviation 3.08
Caregiver Rated Assessment at 1 WeekCaregiver Strain Questionnaire (CGSQ)Global score6.77 score on a scaleStandard Deviation 2.32
Caregiver Rated Assessment at 1 WeekCaregiver Strain Questionnaire (CGSQ)Objective strain2.45 score on a scaleStandard Deviation 0.99
Caregiver Rated Assessment at 1 WeekCaregiver Strain Questionnaire (CGSQ)Subjective internalized strain2.7 score on a scaleStandard Deviation 0.97
Caregiver Rated Assessment at 1 WeekCaregiver Strain Questionnaire (CGSQ)Subjective externalized strain1.62 score on a scaleStandard Deviation 0.69
Secondary

Childrens Sleep Habits Questionnaire

Change in sleep habits at week 1 compared to baseline. Full scale from 0 to 110, with higher score indicating worse health outcomes.

Time frame: Baseline, Week 1

ArmMeasureValue (MEAN)Dispersion
KetamineChildrens Sleep Habits Questionnaire2.83 units on a scaleStandard Deviation 0.75
Caregiver Rated Assessment at 1 WeekChildrens Sleep Habits Questionnaire2.93 units on a scaleStandard Deviation 0.82
Secondary

Clinical Global Impressions - Improvement Scale (CGI-I)

Changes in scale at weeks 2, and 4 compared to baseline. Clinical Global impressions - Improvement Scale is anchored to symptoms of ADNP syndrome for the assessment of treatment effects. CGI-I total score from 1 to 7 point scale, with higher score indicating worse health outcomes.

Time frame: Baseline, Week 2, and Week 4

ArmMeasureGroupValue (MEAN)Dispersion
KetamineClinical Global Impressions - Improvement Scale (CGI-I)Baseline0 score on a scaleStandard Deviation 0
KetamineClinical Global Impressions - Improvement Scale (CGI-I)Week 21.5 score on a scaleStandard Deviation 0.53
KetamineClinical Global Impressions - Improvement Scale (CGI-I)Week 41.0 score on a scaleStandard Deviation 0.52
Secondary

Electrophysiology Recording

Electroencephalographic recordings to measure Auditory Event Related Potentials at baseline, week 1, week 2, and week 4. In separate blocks, participants heard a 500-ms click at either a stimulation rate of 40 or 20 Hz. Click trains were presented 150 times each, with an intertrial interval of 50 ms, at approximately 60 db. Higher number indicates higher amplitude neural response to auditory stimuli.

Time frame: Baseline, Week 1, Week 2, and Week 4

Population: participants with fewer than five wavelets at any time point were excluded

ArmMeasureGroupValue (MEAN)Dispersion
KetamineElectrophysiology Recording20-Hz Baseline0.18 msStandard Deviation 0.06
KetamineElectrophysiology Recording20-Hz Week 10.15 msStandard Deviation 0.05
KetamineElectrophysiology Recording20-Hz Week 20.18 msStandard Deviation 0.06
KetamineElectrophysiology Recording20-Hz Week 40.19 msStandard Deviation 0.11
KetamineElectrophysiology Recording40-Hz Baseline0.19 msStandard Deviation 0.03
KetamineElectrophysiology Recording40-Hz Week10.26 msStandard Deviation 0.09
KetamineElectrophysiology Recording40-Hz Week 20.18 msStandard Deviation 0.06
KetamineElectrophysiology Recording40-Hz Week 40.20 msStandard Deviation 0.06
Secondary

Latency to First Saccade

Change at week 1, week 2, and week 4 as compared to baseline using computerized eye tracking to record where the subject is looking during an activity in which the subject will see different social and non-social stimuli. Latency to first saccade to the target

Time frame: Baseline, Day 1, Week 1

Population: Eye tracking data were successfully collected from nine participants for the Joint Attention task, but only four participants had \>25% valid trials at all three time points and were included in analysis.

ArmMeasureGroupValue (MEAN)Dispersion
KetamineLatency to First SaccadeBaseline2319.38 msStandard Deviation 1202.34
KetamineLatency to First SaccadeDay 12089.96 msStandard Deviation 754.7
KetamineLatency to First SaccadeWeek 11674.18 msStandard Deviation 301.93
Secondary

Peabody Picture Vocabulary Test and Expressive Vocabulary Test

Expressive and receptive language assessed by Peabody Picture Vocabulary Test and Expressive Vocabulary Test at Day 1, Weeks 1, 2, and 4. Full scale from 40 to 160, with higher score indicating better health outcomes.

Time frame: Baseline, Week 1, Week 2, and Week 4

ArmMeasureGroupValue (MEAN)Dispersion
KetaminePeabody Picture Vocabulary Test and Expressive Vocabulary TestBaseline, Day 150.9 score on a scaleStandard Deviation 13.4
KetaminePeabody Picture Vocabulary Test and Expressive Vocabulary TestWeek 152.8 score on a scaleStandard Deviation 17.38
KetaminePeabody Picture Vocabulary Test and Expressive Vocabulary TestWeek 251.5 score on a scaleStandard Deviation 13.87
KetaminePeabody Picture Vocabulary Test and Expressive Vocabulary TestWeek 450.9 score on a scaleStandard Deviation 15.29
Secondary

Proportion of Target-Dwelling

Change at Day 1 and Week 1 as compared to baseline using computerized eye tracking to record where the subject is looking during an activity in which the subject will see different social and non-social stimuli. Proportion of time participants spent dwelling on the target versus distractor.

Time frame: Baseline, Day 1, Week 1

Population: Eye tracking data were successfully collected from nine participants for the Joint Attention task, but only four participants had \>25% valid trials at all three time points and were included in analysis.

ArmMeasureGroupValue (MEAN)Dispersion
KetamineProportion of Target-DwellingBaseline0.51 proportion of timeStandard Deviation 0.19
KetamineProportion of Target-DwellingDay 10.59 proportion of timeStandard Deviation 0.13
KetamineProportion of Target-DwellingWeek 10.66 proportion of timeStandard Deviation 0.11
Secondary

Proportion of Target-First Trials Saccades

Change at Day 1 and Week 1 as compared to baseline using computerized eye tracking to record where the subject is looking during an activity in which the subject will see a video of a person with two objects, turning her head towards one of the objects, the target. Mean proportion of trials in which participants made saccades to the target before the distractor.

Time frame: Baseline, Day 1, Week 1

Population: Not every trial was valid. Eye tracking data were successfully collected from nine participants for the Joint Attention task, but only four participants had \>25% valid trials at all three time points and were included in analysis.

ArmMeasureGroupValue (MEAN)Dispersion
KetamineProportion of Target-First Trials SaccadesBaseline0.53 proportion of target-first saccadesStandard Deviation 0.14
KetamineProportion of Target-First Trials SaccadesDay 10.75 proportion of target-first saccadesStandard Deviation 0.17
KetamineProportion of Target-First Trials SaccadesWeek 10.70 proportion of target-first saccadesStandard Deviation 0.14
Secondary

Repetitive Behavior Scale-Revised (RBS-R)

Change in repetitive behaviors at weeks 1 compared to baseline. RBS-R subscales - Stereo 0-18; Self injury 0-24; Compulsive 0-24; Ritualistic 0-18; Sameness 0-33; Restricted 0-12. Total scale range from 0 to 126 with higher score indicating worse health outcomes.

Time frame: Baseline, Week 1

ArmMeasureGroupValue (MEAN)Dispersion
KetamineRepetitive Behavior Scale-Revised (RBS-R)Compulsive3.7 score on a scaleStandard Deviation 2.75
KetamineRepetitive Behavior Scale-Revised (RBS-R)Sameness5.6 score on a scaleStandard Deviation 6.33
KetamineRepetitive Behavior Scale-Revised (RBS-R)Self-injury5.9 score on a scaleStandard Deviation 4.79
KetamineRepetitive Behavior Scale-Revised (RBS-R)Restricted3.9 score on a scaleStandard Deviation 3.14
KetamineRepetitive Behavior Scale-Revised (RBS-R)Ritualistic2.9 score on a scaleStandard Deviation 3.63
KetamineRepetitive Behavior Scale-Revised (RBS-R)Overall28.6 score on a scaleStandard Deviation 17.56
KetamineRepetitive Behavior Scale-Revised (RBS-R)Stereotyped6.6 score on a scaleStandard Deviation 3.31
Caregiver Rated Assessment at 1 WeekRepetitive Behavior Scale-Revised (RBS-R)Overall22.3 score on a scaleStandard Deviation 14.28
Caregiver Rated Assessment at 1 WeekRepetitive Behavior Scale-Revised (RBS-R)Stereotyped5.1 score on a scaleStandard Deviation 4.93
Caregiver Rated Assessment at 1 WeekRepetitive Behavior Scale-Revised (RBS-R)Self-injury4.2 score on a scaleStandard Deviation 3.49
Caregiver Rated Assessment at 1 WeekRepetitive Behavior Scale-Revised (RBS-R)Compulsive2.2 score on a scaleStandard Deviation 1.87
Caregiver Rated Assessment at 1 WeekRepetitive Behavior Scale-Revised (RBS-R)Ritualistic2.9 score on a scaleStandard Deviation 2.38
Caregiver Rated Assessment at 1 WeekRepetitive Behavior Scale-Revised (RBS-R)Sameness4.3 score on a scaleStandard Deviation 5.46
Caregiver Rated Assessment at 1 WeekRepetitive Behavior Scale-Revised (RBS-R)Restricted3.6 score on a scaleStandard Deviation 2.37
Secondary

Vineland Adaptive Behavior Scales

Changes in scale at week 4 compared to baseline. Vineland Adaptive Behavior Scales measures adaptive functioning. Higher score indicating better health outcomes. Domain scores are standard scores - population mean 100 standard deviation 15. an overall composite score, it consists of three subscales: (a) communication (receptive, expressive, written), (b) socialization (interpersonal relationships, play and leisure, coping skills), and (c) daily living (person, domestic, community).

Time frame: Baseline and Week 4

ArmMeasureGroupValue (MEAN)Dispersion
KetamineVineland Adaptive Behavior ScalesComm32.6 score on a scaleStandard Deviation 14.73
KetamineVineland Adaptive Behavior ScalesSocial44.5 score on a scaleStandard Deviation 15.62
KetamineVineland Adaptive Behavior ScalesDaily Living48.5 score on a scaleStandard Deviation 14.45
KetamineVineland Adaptive Behavior ScalesMotor51.5 score on a scaleStandard Deviation 8.73
KetamineVineland Adaptive Behavior ScalesAbc42.7 score on a scaleStandard Deviation 13.9
Caregiver Rated Assessment at 1 WeekVineland Adaptive Behavior ScalesMotor49.83 score on a scaleStandard Deviation 4.58
Caregiver Rated Assessment at 1 WeekVineland Adaptive Behavior ScalesAbc44.0 score on a scaleStandard Deviation 15.19
Caregiver Rated Assessment at 1 WeekVineland Adaptive Behavior ScalesComm33.4 score on a scaleStandard Deviation 15.53
Caregiver Rated Assessment at 1 WeekVineland Adaptive Behavior ScalesDaily Living49.2 score on a scaleStandard Deviation 16.14
Caregiver Rated Assessment at 1 WeekVineland Adaptive Behavior ScalesSocial46.8 score on a scaleStandard Deviation 16.9

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026